{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,3,19]],"date-time":"2026-03-19T01:07:14Z","timestamp":1773882434209,"version":"3.50.1"},"reference-count":40,"publisher":"Oxford University Press (OUP)","issue":"2","license":[{"start":{"date-parts":[[2025,4,15]],"date-time":"2025-04-15T00:00:00Z","timestamp":1744675200000},"content-version":"vor","delay-in-days":45,"URL":"https:\/\/creativecommons.org\/licenses\/by-nc\/4.0\/"}],"funder":[{"name":"National Science Foundation (NSF) Plant Genome Research Project","award":["1951819"],"award-info":[{"award-number":["1951819"]}]}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"published-print":{"date-parts":[[2025,3,4]]},"abstract":"<jats:title>Abstract<\/jats:title>\n                  <jats:p>Co-fractionation mass spectrometry (CFMS) enables the discovery of protein complexes and the systems-level analysis of multimer dynamics that facilitate responses to environmental and developmental conditions. A major challenge in CFMS data analysis, and omics approaches in general, is the development of reliable benchmarks for accurate evaluation of prediction methods. CORUM is commonly used as a source of benchmark complexes for protein complex composition predictions; however, its assumption of fully assembled subunit pools often conflicts with size exclusion chromatography (SEC) and interaction predictions from CFMS experiments. To address this, we developed an integrative analysis method that leverages cross-kingdom evolutionary conservation among specific CORUM complexes and high-resolution SEC profile data from cell extracts. The resulting benchmark complexes are supported by statistical significance and consistent sizes between calculated and measured apparent masses. The approach was robust, revealing both conserved and species-specific complexes. Designed specifically for benchmark identification, this method can be applied to any species and used to evaluate protein complex predictions from other studies.<\/jats:p>","DOI":"10.1093\/bib\/bbaf154","type":"journal-article","created":{"date-parts":[[2025,4,11]],"date-time":"2025-04-11T07:43:21Z","timestamp":1744357401000},"source":"Crossref","is-referenced-by-count":4,"title":["Integrating CORUM and co-fractionation mass spectrometry to create enhanced benchmarks for protein complex predictions"],"prefix":"10.1093","volume":"26","author":[{"given":"Pengcheng","family":"Yang","sequence":"first","affiliation":[{"name":"Department of Statistics, Purdue University , 150 N. University Street, West Lafayette, IN 47907 ,","place":["USA"]}]},{"given":"Youngwoo","family":"Lee","sequence":"additional","affiliation":[{"name":"Department of Botany and Plant Pathology, Purdue University , 915 Mitch Daniel Blvd., West Lafayette, IN 47907 ,","place":["USA"]},{"name":"Center for Plant Biology, Purdue University , 915 Mitch Daniel Blvd., West Lafayette, IN 47907 ,","place":["USA"]}]},{"given":"Daniel B","family":"Szymanski","sequence":"additional","affiliation":[{"name":"Department of Botany and Plant Pathology, Purdue University , 915 Mitch Daniel Blvd., West Lafayette, IN 47907 ,","place":["USA"]},{"name":"Center for Plant Biology, Purdue University , 915 Mitch Daniel Blvd., West Lafayette, IN 47907 ,","place":["USA"]},{"name":"Department of Biological Sciences, Purdue University , 915 Mitch Daniel Blvd., West Lafayette, IN 47907 ,","place":["USA"]}]},{"given":"Jun","family":"Xie","sequence":"additional","affiliation":[{"name":"Department of Statistics, Purdue University , 150 N. 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